ENST00000340855.11:c.418+59T>G
MANE Select
|
ENSP00000339801.6:n.418+59T>G
|
|
ENST00000651111.1:c.-215-2216T>G
|
ENSP00000498395.1:n.-215-2216T>G
|
|
ENST00000340855.10:c.418+59T>G
|
ENSP00000339801.6:n.418+59T>G
|
|
ENST00000370441.8:c.418+59T>G
|
ENSP00000359470.4:n.418+59T>G
|
|
ENST00000422081.6:c.-215-2216T>G
|
ENSP00000477056.1:n.-215-2216T>G
|
|
ENST00000427113.2:n.770-1030T>G
|
|
|
ENST00000428056.6:c.477T>G
|
ENSP00000390241.2:p.Ile159Met
|
|
ENST00000441880.1:n.114-16155T>G
|
|
|
ENST00000464251.5:c.241+59T>G
|
ENSP00000428980.1:n.241+59T>G
|
|
ENST00000466323.5:c.418+59T>G
|
ENSP00000418264.1:n.418+59T>G
|
|
ENST00000490775.5:n.77+59T>G
|
|
|
ENST00000523759.5:n.533-2216T>G
|
|
|
NM_000202.6:c.418+59T>G
|
NP_000193.1:n.418+59T>G
|
|
NM_001166550.2:c.148+59T>G
|
NP_001160022.1:n.148+59T>G
|
|
NM_006123.4:c.418+59T>G
|
NP_006114.1:n.418+59T>G
|
|
NR_104128.1:n.635+59T>G
|
|
|
NM_000202.7:c.418+59T>G
|
NP_000193.1:n.418+59T>G
|
|
NM_001166550.3:c.148+59T>G
|
NP_001160022.1:n.148+59T>G
|
|
NM_000202.8:c.418+59T>G
MANE Select
|
NP_000193.1:n.418+59T>G
|
|
NM_001166550.4:c.148+59T>G
|
NP_001160022.1:n.148+59T>G
|
|
NM_006123.5:c.418+59T>G
|
NP_006114.1:n.418+59T>G
|
|
NR_104128.2:n.587+59T>G
|
|
|